Autoradiographic detection of mucopolysaccharide accumulation in single fibroblasts

Abstract

A method is described for localizing acid mucopolysaccharides autoradiographically in cultured cells. Normal fibroblasts and fibroblasts, from patients suffering from Mucopolysaccharidosis II disease (MPS II), were cultured for six days in the presence of³⁵SO₄ and one day in unlabelled medium. The cultured cells were transferred to a plastic film dish and, after settling, they were rapidly quenched, freeze-dried, fixed in osmium tetroxide vapour and embedded in Epon. Grain counting after autoradiography in 2 μm sections revealed a significant difference (P>0.001)iin³⁵SO₄ incorporation in the perinuclear cytoplasm of MPS II cells and control cells grown under the same conditions. Autoradiography was also performed after mixing MPS II cells and control fibroblasts in a ratio 1∶1. 8 prior to freezing and the same ratio was found between labelled and unlabelled fibroblasts. These results demonstrate the feasibility of the present autordiographic technique for the detection of the acid mucopolysaccharide storage at the single cell level.